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Impurity reference standards

Lercanidipine impurity standards

This page brings together 30 Lercanidipine related compounds that analytical teams use to identify, quantify and control impurities in the active ingredient and the finished dosage form. The range includes 1 pharmacopoeial impurity and 1 metabolite or hydroxylated analogue.

30reference materials
1pharmacopoeial
1metabolites
Lercanidipine structure
Parent API

Lercanidipine

CAS
100427-26-7
Formula
C36H41N3O6
MW
611.7 g/mol
Code
ZX-006607

Batches are supplied with a certificate of analysis, and the supporting spectra can be sent ahead of a purchase order so your QA team can review them. Typical uses are method development and validation, relative response factor work, forced degradation studies and the impurity sections of ANDA, DMF or CEP filings.

By impurity type

Pharmacopoeial1EP, USP, BP or JP named impurities
Metabolites1Hydroxy, desmethyl and conjugated forms

Counts are based on product names. One compound can fall into more than one type.

All Lercanidipine reference materials

1–30 of 30 standards
Questions

Lercanidipine impurities, answered

What Lercanidipine reference materials are available?
The catalogue currently lists 30 compounds for Lercanidipine, including 1 pharmacopoeial impurity and 1 metabolite or hydroxylated analogue. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Lercanidipine impurity standard?
A certificate of analysis travels with every lot. On request we share the characterisation set, usually 1H-NMR, mass spectrum, HPLC purity and IR, and for some materials TGA or water content. Ask for the data before ordering if your QA team needs to review it.
Can Zemixal make a Lercanidipine impurity that is not listed?
Often yes. Send the structure, name or CAS number with the quantity you need and our sourcing team checks custom synthesis options, usually from 10 mg up to gram scale, with a quoted lead time.
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